53405-0008 NDC - E.O.L. (STILLINGIA SYLVATICA, ZINCUM GLUCONICUM, THIAMINUM HYDROCHLORICUM, FRAGARIA VESCA, NICOTINAMIDUM, RHEUM (PALMATUM), SEROTONIN (HYDROCHLORIDE), 5-HYDROXYTRYPTOPHAN, BETAINUM MURIATICUM, BIOTIN, CHOLINUM, CYSTEINUM, DL-METHIONINE, L-ALANINE, L-CYSTINE, L-GLUTAMIC ACID, L-GLUTAMINE, L-LYSINE, L-METHIONINE, L-SERINE, PARA-AMINOBENZOIC ACID, POTASSIUM GLUCONATE, THYMUS (SUIS), THYROIDINUM (SUIS), UBIDECARENONUM, VITAMIN D3, DOPAMINE HYDROCHLORIDE, LITHIUM BROMATUM, SQUALENE, VACCINIUM MACROCARPON, OXYTOCIN,)

Drug Information

Product NDC: 53405-0008

Proprietary Name: E.O.L.

Non Proprietary Name: Stillingia Sylvatica, Zincum Gluconicum, Thiaminum Hydrochloricum, Fragaria Vesca, Nicotinamidum, Rheum (Palmatum), Serotonin (Hydrochloride), 5-Hydroxytryptophan, Betainum Muriaticum, Biotin, Cholinum, Cysteinum, DL-Methionine, L-Alanine, L-Cystine, L-Glutamic Acid, L-Glutamine, L-Lysine, L-Methionine, L-Serine, Para-Aminobenzoic Acid, Potassium Gluconate, Thymus (Suis), Thyroidinum (Suis), Ubidecarenonum, Vitamin D3, Dopamine Hydrochloride, Lithium Bromatum, Squalene, Vaccinium Macrocarpon, Oxytocin,

Active Ingredient(s):
  • 30 [hp_C]/mL AESCULUS HIPPOCASTANUM FLOWER;
  • 6 [hp_X]/mL ALANINE;
  • 6 [hp_X]/mL AMINOBENZOIC ACID;
  • 6 [hp_X]/mL BETAINE HYDROCHLORIDE;
  • 6 [hp_X]/mL BIOTIN;
  • 12 [hp_X]/mL BORRELIA BURGDORFERI;
  • 6 [hp_C]/mL BROMELAINS;
  • 12 [hp_X]/mL CANDIDA ALBICANS;
  • 6 [hp_X]/mL CHOLECALCIFEROL;
  • 6 [hp_X]/mL CHOLINE HYDROXIDE;
  • 12 [hp_X]/mL COCONUT OIL;
  • 8 [hp_X]/mL COPPER;
  • 7 [hp_X]/mL CRANBERRY;
  • 6 [hp_X]/mL CYSTEINE;
  • 6 [hp_X]/mL CYSTINE;
  • 7 [hp_X]/mL DOPAMINE HYDROCHLORIDE;
  • 5 [hp_X]/mL FRAGARIA VESCA FRUIT;
  • 6 [hp_X]/mL GLUTAMIC ACID;
  • 6 [hp_X]/mL GLUTAMINE;
  • 9 [hp_C]/mL HIPPEASTRUM PUNICEUM WHOLE;
  • 30 [hp_C]/mL ILEX AQUIFOLIUM FLOWERING TOP;
  • 18 [hp_X]/mL LEMON JUICE;
  • 7 [hp_X]/mL LITHIUM BROMIDE;
  • 6 [hp_X]/mL LYSINE;
  • 30 [hp_C]/mL MALUS DOMESTICA FLOWER;
  • 6 [hp_X]/mL METHIONINE;
  • 5 [hp_X]/mL NIACINAMIDE;
  • 6 [hp_X]/mL OXITRIPTAN;
  • 16 [hp_X]/mL OXYTOCIN;
  • 8 [hp_X]/mL PHENYLALANINE;
  • 6 [hp_X]/mL POTASSIUM GLUCONATE;
  • 17 [hp_X]/mL PUMPKIN SEED;
  • 6 [hp_X]/mL RACEMETHIONINE;
  • 5 [hp_X]/mL RHEUM PALMATUM ROOT;
  • 8 [hp_X]/mL SELENIUM;
  • 8 [hp_X]/mL SELENIUM DIOXIDE;
  • 6 [hp_X]/mL SERINE;
  • 5 [hp_X]/mL SEROTONIN HYDROCHLORIDE;
  • 7 [hp_X]/mL SQUALENE;
  • 3 [hp_X]/mL STILLINGIA SYLVATICA ROOT;
  • 6 [hp_X]/mL SUS SCROFA THYMUS;
  • 6 [hp_X]/mL SUS SCROFA THYROID;
  • 4 [hp_X]/mL THIAMINE HYDROCHLORIDE;
  • 6 [hp_X]/mL UBIDECARENONE;
  • 3 [hp_X]/mL ZINC GLUCONATE


Administration Route(s): ORAL

Dosage Form(s): SPRAY

Pharmacy Class(es):
  • Allergens [CS];
  • Allergens [CS];
  • Amino Acid [EPC];
  • Amino Acid [EPC];
  • Amino Acids [CS];
  • Amino Acids [CS];
  • Catecholamine [EPC];
  • Catecholamines [CS];
  • Cell-mediated Immunity [PE];
  • Cell-mediated Immunity [PE];
  • Copper Absorption Inhibitor [EPC];
  • Copper [CS];
  • Copper-containing Intrauterine Device [EPC];
  • Decreased Copper Ion Absorption [PE];
  • Decreased Embryonic Implantation [PE];
  • Decreased Sperm Motility [PE];
  • Dietary Proteins [CS];
  • Fruit Proteins [EXT];
  • Fungal Proteins [CS];
  • Increased Histamine Release [PE];
  • Increased Histamine Release [PE];
  • Increased IgG Production [PE];
  • Increased Large Intestinal Motility [PE];
  • Increased Uterine Smooth Muscle Contraction or Tone [PE];
  • Inhibit Ovum Fertilization [PE];
  • Inhibition Large Intestine Fluid/Electrolyte Absorption [PE];
  • Methylating Activity [MoA];
  • Methylating Agent [EPC];
  • Mood Stabilizer [EPC];
  • Non-Standardized Food Allergenic Extract [EPC];
  • Non-Standardized Fungal Allergenic Extract [EPC];
  • Non-Standardized Plant Allergenic Extract [EPC];
  • Osmotic Activity [MoA];
  • Osmotic Laxative [EPC];
  • Oxytocic [EPC];
  • Oxytocin [CS];
  • Plant Proteins [CS];
  • Potassium Compounds [CS];
  • Potassium Salt [EPC];
  • Vitamin B Complex Member [EPC];
  • Vitamin B Complex [CS];
  • Vitamin D [CS];
  • Vitamin D [EPC]

Labeler Information

Labeler Name: InLight Creation, LLC.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:12/6/2021

Package Information

No. Package Code Package Description Billing Unit
153405-0008-160 mL in 1 BOTTLE, SPRAY (53405-0008-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC53405-0008The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMEE.O.L.The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEStillingia Sylvatica, Zincum Gluconicum, Thiaminum Hydrochloricum, Fragaria Vesca, Nicotinamidum, Rheum (Palmatum), Serotonin (Hydrochloride), 5-Hydroxytryptophan, Betainum Muriaticum, Biotin, Cholinum, Cysteinum, DL-Methionine, L-Alanine, L-Cystine, L-Glutamic Acid, L-Glutamine, L-Lysine, L-Methionine, L-Serine, Para-Aminobenzoic Acid, Potassium Gluconate, Thymus (Suis), Thyroidinum (Suis), Ubidecarenonum, Vitamin D3, Dopamine Hydrochloride, Lithium Bromatum, Squalene, Vaccinium Macrocarpon, Oxytocin,The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMESPRAYThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE12/6/2021This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAMEInLight Creation, LLC.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEAESCULUS HIPPOCASTANUM FLOWER; ALANINE; AMINOBENZOIC ACID; BETAINE HYDROCHLORIDE; BIOTIN; BORRELIA BURGDORFERI; BROMELAINS; CANDIDA ALBICANS; CHOLECALCIFEROL; CHOLINE HYDROXIDE; COCONUT OIL; COPPER; CRANBERRY; CYSTEINE; CYSTINE; DOPAMINE HYDROCHLORIDE; FRAGARIA VESCA FRUIT; GLUTAMIC ACID; GLUTAMINE; HIPPEASTRUM PUNICEUM WHOLE; ILEX AQUIFOLIUM FLOWERING TOP; LEMON JUICE; LITHIUM BROMIDE; LYSINE; MALUS DOMESTICA FLOWER; METHIONINE; NIACINAMIDE; OXITRIPTAN; OXYTOCIN; PHENYLALANINE; POTASSIUM GLUCONATE; PUMPKIN SEED; RACEMETHIONINE; RHEUM PALMATUM ROOT; SELENIUM; SELENIUM DIOXIDE; SERINE; SEROTONIN HYDROCHLORIDE; SQUALENE; STILLINGIA SYLVATICA ROOT; SUS SCROFA THYMUS; SUS SCROFA THYROID; THIAMINE HYDROCHLORIDE; UBIDECARENONE; ZINC GLUCONATEAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH30; 6; 6; 6; 6; 12; 6; 12; 6; 6; 12; 8; 7; 6; 6; 7; 5; 6; 6; 9; 30; 18; 7; 6; 30; 6; 5; 6; 16; 8; 6; 17; 6; 5; 8; 8; 6; 5; 7; 3; 6; 6; 4; 6; 3 
ACTIVE INGRED UNIT[hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL 
PHARM CLASSESAllergens [CS], Allergens [CS], Amino Acid [EPC], Amino Acid [EPC], Amino Acids [CS], Amino Acids [CS], Catecholamine [EPC], Catecholamines [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Copper Absorption Inhibitor [EPC], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Copper Ion Absorption [PE], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Dietary Proteins [CS], Fruit Proteins [EXT], Fungal Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased Large Intestinal Motility [PE], Increased Uterine Smooth Muscle Contraction or Tone [PE], Inhibit Ovum Fertilization [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Methylating Activity [MoA], Methylating Agent [EPC], Mood Stabilizer [EPC], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Fungal Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Osmotic Activity [MoA], Osmotic Laxative [EPC], Oxytocic [EPC], Oxytocin [CS], Plant Proteins [CS], Potassium Compounds [CS], Potassium Salt [EPC], Vitamin B Complex Member [EPC], Vitamin B Complex [CS], Vitamin D [CS], Vitamin D [EPC] 

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This page was last updated on: 2/1/2023